Azobenzene-based unnatural amino acid scaffolds via a Pd(ii)-catalyzed C(sp3)–H arylation strategy. Issue 93 (2nd November 2022)
- Record Type:
- Journal Article
- Title:
- Azobenzene-based unnatural amino acid scaffolds via a Pd(ii)-catalyzed C(sp3)–H arylation strategy. Issue 93 (2nd November 2022)
- Main Title:
- Azobenzene-based unnatural amino acid scaffolds via a Pd(ii)-catalyzed C(sp3)–H arylation strategy
- Authors:
- Tomar, Radha
Suwasia, Sonam
Choudhury, Angshuman Roy
Venkataramani, Sugumar
Babu, Srinivasarao Arulananda - Abstract:
- Abstract : Azobenzene-based unnatural amino acid motifs were constructed via the Pd(ii )-catalyzed diastereoselective β-C(sp 3 )–H arylation and Mills azo coupling tactics. Abstract : Azobenzene-based unnatural amino acid motifs were synthesized via Pd(ii )-catalyzed diastereoselective C(sp 3 )–H arylation of amino acid carboxamides with iodoacetanilides and Mills azo coupling.
- Is Part Of:
- Chemical communications. Volume 58:Issue 93(2022)
- Journal:
- Chemical communications
- Issue:
- Volume 58:Issue 93(2022)
- Issue Display:
- Volume 58, Issue 93 (2022)
- Year:
- 2022
- Volume:
- 58
- Issue:
- 93
- Issue Sort Value:
- 2022-0058-0093-0000
- Page Start:
- 12967
- Page End:
- 12970
- Publication Date:
- 2022-11-02
- Subjects:
- Chemistry -- Periodicals
540 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/cc ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d2cc04870a ↗
- Languages:
- English
- ISSNs:
- 1359-7345
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3139.350000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 24359.xml